High levels of SARS-CoV-2–specific T cells with restricted functionality in severe courses of COVID-19
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SciScore for 10.1101/2020.07.08.20148718: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: The study was approved by the ethics committee of the Ärztekammer des Saarlandes (references 76/20; l62/20) and all individuals or their legal representatives gave written informed consent.
Consent: The study was approved by the ethics committee of the Ärztekammer des Saarlandes (references 76/20; l62/20) and all individuals or their legal representatives gave written informed consent.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources Quantitation of lymphocyte populations: Quantitation and characterization of lymphocyte subpopulations was … SciScore for 10.1101/2020.07.08.20148718: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Institutional Review Board Statement IRB: The study was approved by the ethics committee of the Ärztekammer des Saarlandes (references 76/20; l62/20) and all individuals or their legal representatives gave written informed consent.
Consent: The study was approved by the ethics committee of the Ärztekammer des Saarlandes (references 76/20; l62/20) and all individuals or their legal representatives gave written informed consent.Randomization not detected. Blinding not detected. Power Analysis not detected. Sex as a biological variable not detected. Table 2: Resources
Antibodies Sentences Resources Quantitation of lymphocyte populations: Quantitation and characterization of lymphocyte subpopulations was performed on 100 µL of heparinized whole blood as described before 36 using monoclonal antibodies towards CD3 (clone SK7), CD4 (clone SK3), CD8 (clone RPA-T8 and SK1), CD16 (clone 3G8), CD19 (clone HIB19), CD27 (clone L128), CD38 (clone HB7), CD56 (clone B159), cytotoxic T lymphocyte antigen 4 (CTLA-4, clone BNI3), IgD (clone IA6-2) and programmed cell death 1 (PD-1, clone MIH4, all from BD Biosciences). CD4suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)CD8suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)CD16suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)CD19suggested: (BD Biosciences Cat# 557939, RRID:AB_2802162)CD38suggested: (RayBiotech Cat# CS-11-0123, RRID:AB_1228026)CTLA-4suggested: NoneIgDsuggested: NonePD-1suggested: NoneDifferentiation status of CD19-positive B-cells was assessed using antibodies against IgD and CD27. antibodies against IgDsuggested: NoneCD27suggested: NoneNK cells were identified using antibodies towards CD3, CD16 and CD56 and quantified as CD3 negative/CD16/CD56 positive lymphocytes. CD3suggested: NoneCD56suggested: NoneAnalysis of SARS-CoV-2 specific antibodies: SARS-CoV-2 specific antibodies were quantified from heparinized plasma samples using an IgG and IgA assay coated with recombinant S1-domain of SARS-CoV-2 spike protein antigen according to the manufacturer’s instructions (Euroimmun, Lübeck, Germany). SARS-CoV-2 spike proteinsuggested: NoneAn unpaired non-parametric Kruskall-Wallis test with Dunn’s post test was used to analyze differences for lymphocyte subpopulations, T-cell and antibody levels as wells as PD-1, CTLA-4 and Ki67 of total T-cells among the three groups. PD-1, CTLA-4suggested: (Thermo Fisher Scientific Cat# EPX140-15803-901, RRID:AB_2576106)Software and Algorithms Sentences Resources Statistical analysis: Statistical analysis was carried out using GraphPad Prism 8.0 software using two-tailed tests. GraphPad Prismsuggested: (GraphPad Prism, RRID:SCR_002798)Results from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.Results from TrialIdentifier: No clinical trial numbers were referenced.
Results from Barzooka: We found bar graphs of continuous data. We recommend replacing bar graphs with more informative graphics, as many different datasets can lead to the same bar graph. The actual data may suggest different conclusions from the summary statistics. For more information, please see Weissgerber et al (2015).
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
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